We anticipate the application window for this opening will close on - 13 Jun 2025

 

At Medtronic you can begin a life-long career of exploration and innovation, while helping champion healthcare access and equity for all. You’ll lead with purpose, breaking down barriers to innovation in a more connected, compassionate world.

A Day in the Life

This Production Coordinator III will work under general supervision to perform diversified duties such as implementing product Bill of Materials (BOM) and manufacturing flow configurations in a Manufacturing Execution System (MES) to ensure that product traceability are accurately captured in MES to meet FDA compliance requirements. This Production Coordinator III will also maintain documentation of department policies and procedures and ensure compliance with FDA and Medtronic Quality Systems. During quality issues, the MES Coordinator may perform data mining to identify suspect materials and coordinates with production to contain suspect materials by executing Quality Holds in FACTORYworks.

A career at Medtronic is like no other. We’re purposeful. We’re committed. And we’re driven by our Mission to alleviate pain, restore health and extend life for millions of people worldwide. 

A Day in the Life

This Production Coordinator III will work under general supervision to perform diversified duties such as implementing product Bill of Materials (BOM) and manufacturing flow configurations in a Manufacturing Execution System (MES) to ensure that product traceability are accurately captured in MES to meet FDA compliance requirements. This Production Coordinator III will also maintain documentation of department policies and procedures and ensure compliance with FDA and Medtronic Quality Systems. During quality issues, the MES Coordinator may perform data mining to identify suspect materials and coordinates with production to contain suspect materials by executing Quality Holds in FACTORYworks.  

MES PRODUCTION COORDINATOR III

Responsibilities include, but are not limited to:

• Configure the Product, product BOM, manufacturing flow, and build profile in MES based on product specifications to support Hybrid, IC Test, Die Prep (ICDP), Diabetes and Wafer Scale Operations (WSO) across entire Medtronic Tempe Campus

• Review production specifications and documentation to configure systems: MES (FACTORYworks), ChemTrace, Loftware or other MES Labeling system, LIMS6, LIMS7, & LIMS8 (IPSU – Inspection Procedure Set Up) to support manufacturing

• Collaborate with engineers/technicians on equipment change (ECA), task management (MEST) and engineering data collection (MESDC) documents to setup equipment configurations, tasks and engineering data collection in FACTORYworks

• Collaborate with engineers/technicians for FACTORYworks configuration of RCCs (Reason Code Change), PFRs (Product File Request), RETMs (External Foundry IC Reticle Set) & SPC (Statistical Process Control), MPDC (Manufacturing Process Development Checklist).

• Collaborate with submitters for FACTORYworks lot updates with LTC (Lot Type Changes), PNC (Product_Part Number Changes), RMF (Reinstate Material Form), EMPE (ESD Mishandled Predisposition Evaluation), & PPDRs (Product/Process Disposition Report).

• Collaborate with engineering and sourcing team on setting up off-site processing flow per product specifications.

• Collaborate with Manufacturing Operations to correct tracking errors through MES Request System.

• Perform device data mining to create device lot list to support quality issue investigation. Collaborate with engineering and Quality Assurance (QA) teams to identify suspect device lots and coordinate with Planning and Ops teams to isolate non-conforming product during containment and assist in opening/closing Quality Holds

• Update DHR based on Non-Conforming Report (NCR) to support non-conforming product disposition and implement appropriate system corrective action as needed to address NCR per MES Requests.

• Run various MES data extracts as required to support engineering evaluation or process improvement projects

• Provide Device History Record (DHR) to support audit activities

• Review manufacturing specifications and process documentation and ensures compliance with FDA regulations and MDT internal quality policies

• Collaborate with Product Development team on system enhancements needed to support the introduction of new manufacturing processes/products

• Understand Document Repository systems (